HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 17173Generated: October 25, 2026
Ammonium Chloride → (S)-N-Boc-2-ethynylpyrrolidine
https://huagongshe.com/reaction/17173
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | (S)-t-butyl 2-(2,2-dibromovinyl)pyrrolidine-1-carboxylate | HCID 14730281 | — |
| Reactant | CID 53628100 | HCID 178418400 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | (S)-N-Boc-2-ethynylpyrrolidine | HCID 11030701 | — |
Reaction Steps
A solution of Example 538A (6.11 g, 17.21 mmol) in THF (150 mL) at −78° C. was treated with sec-butyl lithium (24.6 mL, 34.41 mmol) dropwise via syringe and stirred for 30 minutes at −78° C. The solution was then treated with a saturated ammonium chloride solution (100 mL), allowed to warm to room temperature, diluted with ether and extracted. The combined organic layers were washed with brine, dried (MgSO4) and concentrated to provide the desired product in quantitative yield. MS (ESI(+)) m/e 196 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07737160B2 |
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| Source dataset | uspto-grants-2010_06 |
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| ORD ID | ord-3b7925b1660d4f6187f302317a8f9746 |
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| Source note | uspto-grants-2010_06 |
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